Does LUBIPROSTONE Cause Incorrect dose administered? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Incorrect dose administered have been filed in association with LUBIPROSTONE (Amitza). This represents 1.3% of all adverse event reports for LUBIPROSTONE.
16
Reports of Incorrect dose administered with LUBIPROSTONE
1.3%
of all LUBIPROSTONE reports
3
Deaths
5
Hospitalizations
How Dangerous Is Incorrect dose administered From LUBIPROSTONE?
Of the 16 reports, 3 (18.8%) resulted in death, 5 (31.3%) required hospitalization.
Is Incorrect dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does LUBIPROSTONE Cause?
Diarrhoea (170)
Drug ineffective (131)
Nausea (110)
Constipation (82)
Vomiting (75)
Dizziness (59)
Abdominal distension (57)
Dyspnoea (53)
Headache (47)
Abdominal pain (45)
What Other Drugs Cause Incorrect dose administered?
TIRZEPATIDE (23,301)
ADALIMUMAB (14,000)
DUPILUMAB (9,907)
RANITIDINE (9,337)
INSULIN LISPRO (8,318)
ACETAMINOPHEN (5,316)
DULAGLUTIDE (5,207)
SECUKINUMAB (4,524)
INSULIN GLARGINE (3,070)
SOMATROPIN (2,772)
Which LUBIPROSTONE Alternatives Have Lower Incorrect dose administered Risk?
LUBIPROSTONE vs LUCENTIS
LUBIPROSTONE vs LUCRIN DEPOT
LUBIPROSTONE vs LUMASIRAN
LUBIPROSTONE vs LUMATEPERONE
LUBIPROSTONE vs LUMIGAN